Senoj Biocare, Inc.
Country not established
- Devices
- 1
What Senoj Biocare, Inc. makes
Senoj Biocare, Inc. manufactures the SENOJ Implant System, a medical device designed for soft tissue augmentation or reconstruction.
The SENOJ Implant System is classified as a Class II device under FDA regulations and is listed in the FDA’s 510(k) clearance registry. The company is based in the United States.
Catalogue
Senoj Implant System Ref K000889
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Senoj Biocare, Inc. have in the registry?
The registry currently lists 1 device for Senoj Biocare, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Senoj Biocare, Inc.'s devices?
Among its 1 most recently registered device, Senoj Biocare, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Senoj Biocare, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Senoj Biocare, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Senoj Biocare, Inc. in the registry?
The most recently registered devices listed for Senoj Biocare, Inc. include SENOJ IMPLANT SYSTEM.